Serveur d'exploration Phytophthora

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Next-generation sequencing to identify candidate genes and develop diagnostic markers for a novel Phytophthora resistance gene, RpsHC18, in soybean.

Identifieur interne : 000712 ( Main/Exploration ); précédent : 000711; suivant : 000713

Next-generation sequencing to identify candidate genes and develop diagnostic markers for a novel Phytophthora resistance gene, RpsHC18, in soybean.

Auteurs : Chao Zhong [République populaire de Chine] ; Suli Sun [République populaire de Chine] ; Yinping Li [République populaire de Chine] ; Canxing Duan [République populaire de Chine] ; Zhendong Zhu [République populaire de Chine]

Source :

RBID : pubmed:29138903

Descripteurs français

English descriptors

Abstract

KEY MESSAGE

A novel Phytophthora sojae resistance gene RpsHC18 was identified and finely mapped on soybean chromosome 3. Two NBS-LRR candidate genes were identified and two diagnostic markers of RpsHC18 were developed. Phytophthora root rot caused by Phytophthora sojae is a destructive disease of soybean. The most effective disease-control strategy is to deploy resistant cultivars carrying Phytophthora-resistant Rps genes. The soybean cultivar Huachun 18 has a broad and distinct resistance spectrum to 12 P. sojae isolates. Quantitative trait loci sequencing (QTL-seq), based on the whole-genome resequencing (WGRS) of two extreme resistant and susceptible phenotype bulks from an F


DOI: 10.1007/s00122-017-3016-z
PubMed: 29138903


Affiliations:


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Le document en format XML

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<term>Base Sequence (MeSH)</term>
<term>Chromosome Mapping (MeSH)</term>
<term>Disease Resistance (genetics)</term>
<term>Genes, Plant (MeSH)</term>
<term>Genetic Markers (MeSH)</term>
<term>High-Throughput Nucleotide Sequencing (MeSH)</term>
<term>INDEL Mutation (MeSH)</term>
<term>Microsatellite Repeats (MeSH)</term>
<term>Phenotype (MeSH)</term>
<term>Phytophthora (MeSH)</term>
<term>Plant Diseases (genetics)</term>
<term>Plant Diseases (microbiology)</term>
<term>Polymorphism, Single Nucleotide (MeSH)</term>
<term>Quantitative Trait Loci (MeSH)</term>
<term>Soybeans (genetics)</term>
<term>Soybeans (microbiology)</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr">
<term>Cartographie chromosomique (MeSH)</term>
<term>Gènes de plante (MeSH)</term>
<term>Locus de caractère quantitatif (MeSH)</term>
<term>Maladies des plantes (génétique)</term>
<term>Maladies des plantes (microbiologie)</term>
<term>Marqueurs génétiques (MeSH)</term>
<term>Mutation de type INDEL (MeSH)</term>
<term>Phytophthora (MeSH)</term>
<term>Phénotype (MeSH)</term>
<term>Polymorphisme de nucléotide simple (MeSH)</term>
<term>Répétitions microsatellites (MeSH)</term>
<term>Résistance à la maladie (génétique)</term>
<term>Soja (génétique)</term>
<term>Soja (microbiologie)</term>
<term>Séquence nucléotidique (MeSH)</term>
<term>Séquençage nucléotidique à haut débit (MeSH)</term>
</keywords>
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<term>Genetic Markers</term>
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<term>Disease Resistance</term>
<term>Plant Diseases</term>
<term>Soybeans</term>
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<term>Maladies des plantes</term>
<term>Résistance à la maladie</term>
<term>Soja</term>
</keywords>
<keywords scheme="MESH" qualifier="microbiologie" xml:lang="fr">
<term>Maladies des plantes</term>
<term>Soja</term>
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<term>Plant Diseases</term>
<term>Soybeans</term>
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<term>Base Sequence</term>
<term>Chromosome Mapping</term>
<term>Genes, Plant</term>
<term>High-Throughput Nucleotide Sequencing</term>
<term>INDEL Mutation</term>
<term>Microsatellite Repeats</term>
<term>Phenotype</term>
<term>Phytophthora</term>
<term>Polymorphism, Single Nucleotide</term>
<term>Quantitative Trait Loci</term>
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<term>Cartographie chromosomique</term>
<term>Gènes de plante</term>
<term>Locus de caractère quantitatif</term>
<term>Marqueurs génétiques</term>
<term>Mutation de type INDEL</term>
<term>Phytophthora</term>
<term>Phénotype</term>
<term>Polymorphisme de nucléotide simple</term>
<term>Répétitions microsatellites</term>
<term>Séquence nucléotidique</term>
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<b>KEY MESSAGE</b>
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<p>A novel Phytophthora sojae resistance gene RpsHC18 was identified and finely mapped on soybean chromosome 3. Two NBS-LRR candidate genes were identified and two diagnostic markers of RpsHC18 were developed. Phytophthora root rot caused by Phytophthora sojae is a destructive disease of soybean. The most effective disease-control strategy is to deploy resistant cultivars carrying Phytophthora-resistant Rps genes. The soybean cultivar Huachun 18 has a broad and distinct resistance spectrum to 12 P. sojae isolates. Quantitative trait loci sequencing (QTL-seq), based on the whole-genome resequencing (WGRS) of two extreme resistant and susceptible phenotype bulks from an F</p>
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<AbstractText Label="KEY MESSAGE" NlmCategory="UNASSIGNED">A novel Phytophthora sojae resistance gene RpsHC18 was identified and finely mapped on soybean chromosome 3. Two NBS-LRR candidate genes were identified and two diagnostic markers of RpsHC18 were developed. Phytophthora root rot caused by Phytophthora sojae is a destructive disease of soybean. The most effective disease-control strategy is to deploy resistant cultivars carrying Phytophthora-resistant Rps genes. The soybean cultivar Huachun 18 has a broad and distinct resistance spectrum to 12 P. sojae isolates. Quantitative trait loci sequencing (QTL-seq), based on the whole-genome resequencing (WGRS) of two extreme resistant and susceptible phenotype bulks from an F
<sub>2:3</sub>
population, was performed, and one 767-kb genomic region with ΔSNP-index ≥ 0.9 on chromosome 3 was identified as the RpsHC18 candidate region in Huachun 18. The candidate region was reduced to a 146-kb region by fine mapping. Nonsynonymous SNP and haplotype analyses were carried out in the 146-kb region among ten soybean genotypes using WGRS. Four specific nonsynonymous SNPs were identified in two nucleotide-binding sites-leucine-rich repeat (NBS-LRR) genes, RpsHC18-NBL1 and RpsHC18-NBL2, which were considered to be the candidate genes. Finally, one specific SNP marker in each candidate gene was successfully developed using a tetra-primer ARMS-PCR assay, and the two markers were verified to be specific for RpsHC18 and to effectively distinguish other known Rps genes. In this study, we applied an integrated genomic-based strategy combining WGRS with traditional genetic mapping to identify RpsHC18 candidate genes and develop diagnostic markers. These results suggest that next-generation sequencing is a precise, rapid and cost-effective way to identify candidate genes and develop diagnostic markers, and it can accelerate Rps gene cloning and marker-assisted selection for breeding of P. sojae-resistant soybean cultivars.</AbstractText>
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